2.1.1.231: flavonoid 4'-O-methyltransferase
This is an abbreviated version!
For detailed information about flavonoid 4'-O-methyltransferase, go to the full flat file.
Word Map on EC 2.1.1.231
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2.1.1.231
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quercetin
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4'-o-methylation
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flavone
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naringenin
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luteolin
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saccharopolyspora
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4'-methylated
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flavanones
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acacetin
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rebeccamycin
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rhamnosyl
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kaempferol
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apigenin
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spinosyn
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indolocarbazole
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synthesis
- 2.1.1.231
- quercetin
-
4'-o-methylation
- flavone
- naringenin
- luteolin
-
saccharopolyspora
-
4'-methylated
- flavanones
- acacetin
- rebeccamycin
-
rhamnosyl
- kaempferol
- apigenin
-
spinosyn
-
indolocarbazole
- synthesis
Reaction
Synonyms
4'-O-methyltransferase, 4'OMT, B-ring 4'OMT, F 4'-OMT, flavonoid 4'-O-methyltransferase, GerMIII, O-methyltransferase, OMT, regiospecific flavonoid 4'OMT, SOMT-2, SOMT2, soybean O-methyltransferase
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General Information
General Information on EC 2.1.1.231 - flavonoid 4'-O-methyltransferase
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evolution
GerMIII is present on the biosynthetic gene cluster of dihydrochalcomycin, a macrolide antibiotic that is produced by the Streptomyces sp. KCTC 0041BP. Based on its dependency on the metallic cofactor requirement for its reaction, the enzyme resembles the Class-II plant OMTs
metabolism
the enzyme catalyzes the last step in the biosynthesis of the bioactive flavonoid ponciretin, biosynthetic pathways starting with glucose, overview
physiological function
the methylation at the 4'-hydroxyl group of the B-ring of flavonoids confers a structural constraint for autooxidation, importance of the regiospecific 4'-OMT
additional information
a double bond between the C2 and the C3 and a single-ring-appended conjugate-hydroxyl group are crucial for the favorable enzymatic conversions of the GerMIII catalysis, modeling and molecular docking